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dc.contributor.authorZinovkin, DA
dc.contributor.authorAchinovich, SL
dc.contributor.authorZubritskiy, MG
dc.contributor.authorWhatmore, JL
dc.contributor.authorPranjo, MZI
dc.date.accessioned2019-09-06T08:46:18Z
dc.date.issued2019-06-27
dc.description.abstractBackground: In this study, we investigate the expression of markers of angiogenesis and microvessel density (MVD) in cases of microcystic, elongated and fragmented (MELF) pattern, with its prognostic role in the survival of endometrioid endometrial cancer (EA) patients. Materials and Methods: In this study, 100 cases of EA, 49 cases with MELF pattern and 51 without, were immunohistochemically stained for galectin-1, vascular endothelial growth factor (VEGF), and MVD. Morphometry and statistical (univariate and multivariate) analyses were performed to assess overall survival (OS) and disease-free survival. Results: The expression of VEGF (p<.001) and galectin-1 (p<.001), as well asMVD area (p=.0003) and number of vessels/mm2 (p=.0043), were significantly higher in the +MELF pattern group compared to the -MELF group. A low negative correlation between MELF-pattern and the number of days of survival (p<.001, r=-0.47) was also found. A low positive correlation of MELF-pattern with galectin-1 expression (p<.001, r=0.39), area of vessels/mm2 (p<.001, r=0.36), outcome of EA (p<.001, r = 0.42) and VEGF expression (p<.001, r=0.39) suggests potential pathological relevance of these factors in the prognosis of EA. A univariate survival analysis indicated a role for all parameters of survival. Multivariate Cox proportional hazard regression analysis revealed that only area of vessels/mm2 (hazard ratio [HR], 1.018; 95% confidence interval [CI], 1.002 to 1.033), galectin-1 (HR, 1.049; 95% CI, 1.025 to 1.074) and VEGF (HR, 1.049; 95% CI, 1.022 to 1.077) play key roles in OS. Conclusion: This study reports an increase in MVD, VEGF and galectin-1 expression in EA with MELF pattern and suggests that MELF pattern, along with the angiogenic profile, may be a prognostic factor in EA.en_GB
dc.description.sponsorshipFORCE Cancer Charityen_GB
dc.description.sponsorshipGomel State Medical Universityen_GB
dc.identifier.citationPublished online 27 June 2019en_GB
dc.identifier.doi10.4132/jptm.2019.05.13
dc.identifier.urihttp://hdl.handle.net/10871/38556
dc.language.isoenen_GB
dc.publisherThe Korean Society of Pathologists/The Korean Society for Cytopathologyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/31243940en_GB
dc.rights© The Korean Society of Pathologists/The Korean Society for Cytopathology. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectEndometrioid endometrial carcinomaen_GB
dc.subjectGalectin-1en_GB
dc.subjectMELF patternen_GB
dc.subjectMicrovessel densityen_GB
dc.subjectVEGFen_GB
dc.titleHigh Expression of Galectin-1, VEGF and Increased Microvessel Density are Associated with MELF Pattern in Stage I-III Endometrioid Endometrial Adenocarcinomaen_GB
dc.typeArticleen_GB
dc.date.available2019-09-06T08:46:18Z
dc.identifier.issn2383-7837
exeter.place-of-publicationKorea (South)en_GB
dc.descriptionThis is the final version. Available on open access via the DOI in this recorden_GB
dc.identifier.journalJournal of Pathology and Translational Medicineen_GB
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0en_GB
dcterms.dateAccepted2019-05-13
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2019-06-27
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-09-06T08:44:01Z
refterms.versionFCDVoR
refterms.dateFOA2019-09-06T08:46:21Z
refterms.panelAen_GB
refterms.depositExceptionpublishedGoldOA


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© The Korean Society of Pathologists/The Korean Society for Cytopathology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's licence is described as © The Korean Society of Pathologists/The Korean Society for Cytopathology. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.